Canonical Allele Identifier: CA2754311150
Gene: WNT10A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218893206_218893207insGAA , CM000664.2:g.218893206_218893207insGAA GRCh38
NC_000002.11:g.219757928_219757929insGAA , CM000664.1:g.219757928_219757929insGAA GRCh37
NC_000002.10:g.219466172_219466173insGAA NCBI36
NG_012179.1:g.17674_17675insGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000258411.8:c.1189_1190insGAA MANE Select ENSP00000258411.3:p.His397delinsArgAsn
ENST00000258411.7:c.1189_1190insGAA ENSP00000258411.3:p.His397delinsArgAsn
NM_025216.2:c.1189_1190insGAA NP_079492.2:p.His397delinsArgAsn
XM_011511928.1:c.1138_1139insGAA XP_011510230.1:p.His380delinsArgAsn
XM_011511929.1:c.1093_1094insGAA XP_011510231.1:p.His365delinsArgAsn
XM_011511930.1:c.809_810insGAA XP_011510232.1:p.Pro270_Leu271insLys
XM_011511929.2:c.1093_1094insGAA XP_011510231.1:p.His365delinsArgAsn
NM_025216.3:c.1189_1190insGAA MANE Select NP_079492.2:p.His397delinsArgAsn
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